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Hydrazoic acid

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(Redirected from Hydrogen azide) Unstable and toxic chemical compound
Hydrazoic acid
Structure, bonding and dimensions of the hydrogen azide molecule
Hydrazoic acid
Hydrazoic acid
Names
IUPAC name Hydrogen azide
Other names Hydrogen azide
Azoimide
Azic acid
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.029.059 Edit this at Wikidata
EC Number
  • 231-965-8
Gmelin Reference 773
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/HN3/c1-3-2/h1HKey: JUINSXZKUKVTMD-UHFFFAOYSA-N
  • InChI=1/HN3/c1-3-2/h1HKey: JUINSXZKUKVTMD-UHFFFAOYAO
SMILES
  • ==N
  • N#
Properties
Chemical formula HN3
Molar mass 43.029 g·mol
Appearance colorless, highly volatile liquid
Density 1.09 g/cm
Melting point −80 °C (−112 °F; 193 K)
Boiling point 37 °C (99 °F; 310 K)
Solubility in water highly soluble
Solubility soluble in alkali, alcohol, ether
Acidity (pKa) 4.6
Conjugate base Azide
Structure
Molecular shape approximately linear
Hazards
Occupational safety and health (OHS/OSH):
Main hazards Highly toxic, explosive, reactive
GHS labelling:
Pictograms GHS01: ExplosiveGHS07: Exclamation markGHS08: Health hazard
Signal word Danger
Hazard statements H200, H319, H335, H370
Precautionary statements P201, P202, P260, P261, P264, P270, P271, P280, P281, P304+P340, P305+P351+P338, P307+P311, P312, P321, P337+P313, P372, P373, P380, P401, P403+P233, P405, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 4: Very short exposure could cause death or major residual injury. E.g. VX gasFlammability 0: Will not burn. E.g. waterInstability 3: Capable of detonation or explosive decomposition but requires a strong initiating source, must be heated under confinement before initiation, reacts explosively with water, or will detonate if severely shocked. E.g. hydrogen peroxideSpecial hazards (white): no code
4 0 3
Related compounds
Other cations Sodium azide
Lithium azide
Potassium azide
Related nitrogen hydrides Ammonia
Hydrazine
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

Hydrazoic acid, also known as hydrogen azide, azic acid or azoimide, is a compound with the chemical formula HN3. It is a colorless, volatile, and explosive liquid at room temperature and pressure. It is a compound of nitrogen and hydrogen, and is therefore a pnictogen hydride. It was first isolated in 1890 by Theodor Curtius. The acid has few applications, but its conjugate base, the azide ion, is useful in specialized processes.

Hydrazoic acid, like its fellow mineral acids, is soluble in water. Undiluted hydrazoic acid is dangerously explosive with a standard enthalpy of formation ΔfH (l, 298K) = +264 kJ/mol. When dilute, the gas and aqueous solutions (<10%) can be safely prepared but should be used immediately; because of its low boiling point, hydrazoic acid is enriched upon evaporation and condensation such that dilute solutions incapable of explosion can form droplets in the headspace of the container or reactor that are capable of explosion.

Production

The acid is usually formed by acidification of an azide salt like sodium azide. Normally solutions of sodium azide in water contain trace quantities of hydrazoic acid in equilibrium with the azide salt, but introduction of a stronger acid can convert the primary species in solution to hydrazoic acid. The pure acid may be subsequently obtained by fractional distillation as an extremely explosive colorless liquid with an unpleasant smell.

NaN3 + HCl → HN3 + NaCl

Its aqueous solution can also be prepared by treatment of barium azide solution with dilute sulfuric acid, filtering the insoluble barium sulfate.

It was originally prepared by the reaction of aqueous hydrazine with nitrous acid:

N2H4 + HNO2 → HN3 + 2 H2O

With the hydrazinium cation [N2H5] this reaction is written as:

[N2H5] + HNO2 → HN3 + H2O + [H3O]

Other oxidizing agents, such as hydrogen peroxide, nitrosyl chloride, trichloramine or nitric acid, can also be used to produce hydrazoic acid from hydrazine.

Destruction prior to disposal

Hydrazoic acid reacts with nitrous acid:

HN3 + HNO2 → N2O + N2 + H2O

This reaction is unusual in that it involves compounds with nitrogen in four different oxidation states.

Reactions

In its properties hydrazoic acid shows some analogy to the halogen acids, since it forms poorly soluble (in water) lead, silver and mercury(I) salts. The metallic salts all crystallize in the anhydrous form and decompose on heating, leaving a residue of the pure metal. It is a weak acid (pKa = 4.75.) Its heavy metal salts are explosive and readily interact with the alkyl iodides. Azides of heavier alkali metals (excluding lithium) or alkaline earth metals are not explosive, but decompose in a more controlled way upon heating, releasing spectroscopically-pure N2 gas. Solutions of hydrazoic acid dissolve many metals (e.g. zinc, iron) with liberation of hydrogen and formation of salts, which are called azides (formerly also called azoimides or hydrazoates).

Hydrazoic acid may react with carbonyl derivatives, including aldehydes, ketones, and carboxylic acids, to give an amine or amide, with expulsion of nitrogen. This is called Schmidt reaction or Schmidt rearrangement.

Dissolution in the strongest acids produces explosive salts containing the aminodiazonium ion [H2N=N=N] ⇌ [H2N−N≡N], for example:

HN=N=N + H[SbCl6] → [H2N=N=N][SbCl6]

The ion [H2N=N=N] is isoelectronic to diazomethane H2C=N=N.

The decomposition of hydrazoic acid, triggered by shock, friction, spark, etc. produces nitrogen and hydrogen:

2 HN3 → H2 + 3 N2

Hydrazoic acid undergoes unimolecular decomposition at sufficient energy:

HN3 → NH + N2

The lowest energy pathway produces NH in the triplet state, making it a spin-forbidden reaction. This is one of the few reactions whose rate has been determined for specific amounts of vibrational energy in the ground electronic state, by laser photodissociation studies. In addition, these unimolecular rates have been analyzed theoretically, and the experimental and calculated rates are in reasonable agreement.

Toxicity

Hydrazoic acid is volatile and highly toxic. It has a pungent smell and its vapor can cause violent headaches. The compound acts as a non-cumulative poison.

Applications

2-Furonitrile, a pharmaceutical intermediate and potential artificial sweetening agent has been prepared in good yield by treating furfural with a mixture of hydrazoic acid (HN3) and perchloric acid (HClO4) in the presence of magnesium perchlorate in the benzene solution at 35 °C.

The all gas-phase iodine laser (AGIL) mixes gaseous hydrazoic acid with chlorine to produce excited nitrogen chloride, which is then used to cause iodine to lase; this avoids the liquid chemistry requirements of COIL lasers.

References

  1. Pradyot Patnaik. Handbook of Inorganic Chemicals. McGraw-Hill, 2002, ISBN 0-07-049439-8
  2. ^ Chisholm, Hugh, ed. (1911). "Azoimide" . Encyclopædia Britannica. Vol. 3 (11th ed.). Cambridge University Press. pp. 82–83. This also contains a detailed description of the contemporaneous production process.
  3. Dictionary of Inorganic and Organometallic Compounds. Chapman & Hall.
  4. Curtius, Theodor (1890). "Ueber Stickstoffwasserstoffsäure (Azoimid) N3H" [On hydrazoic acid (azoimide) N3H]. Berichte der Deutschen Chemischen Gesellschaft. 23 (2): 3023–3033. doi:10.1002/cber.189002302232.
  5. Furman, David; Dubnikova, Faina; van Duin, Adri C. T.; Zeiri, Yehuda; Kosloff, Ronnie (2016-03-10). "Reactive Force Field for Liquid Hydrazoic Acid with Applications to Detonation Chemistry". The Journal of Physical Chemistry C. 120 (9): 4744–4752. Bibcode:2016APS..MARH20013F. doi:10.1021/acs.jpcc.5b10812. ISSN 1932-7447. S2CID 102029987.
  6. ^ Catherine E. Housecroft; Alan G. Sharpe (2008). "Chapter 15: The group 15 elements". Inorganic Chemistry, 3rd Edition. Pearson. p. 449. ISBN 978-0-13-175553-6.
  7. Gonzalez-Bobes, F. et al Org. Process Res. Dev. 2012, 16, 2051-2057.
  8. Treitler, D. S. et al Org. Process Res. Dev. 2017, 21, 460-467.
  9. L . F. Audrieth, C. F. Gibbs Hydrogen Azide in Aqueous and Ethereal Solution" Inorganic Syntheses 1939, vol. 1, pp. 71-79.
  10. Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 432. ISBN 978-0-08-037941-8.
  11. Greenwood, pp. 461–464.
  12. ^ Egon Wiberg; Nils Wiberg; Arnold Frederick Holleman (2001). "The Nitrogen Group". Inorganic chemistry. Academic Press. p. 625. ISBN 978-0-12-352651-9.
  13. Foy, B.R.; Casassa, M.P.; Stephenson, J.C.; King, D.S. (1990). "Overtone-excited HN
    3 (X1A') - Anharmonic resonance, homogeneous linewidths, and dissociation rates". Journal of Chemical Physics. 92: 2782–2789. doi:10.1063/1.457924.
  14. Besora, M.; Harvey, J.N. (2008). "Understanding the rate of spin-forbidden thermolysis of HN
    3 and CH
    3N
    3". Journal of Chemical Physics. 129 (4): 044303. doi:10.1063/1.2953697. PMID 18681642.
  15. P. A. Pavlov; Kul'nevich, V. G. (1986). "Synthesis of 5-substituted furannitriles and their reaction with hydrazine". Khimiya Geterotsiklicheskikh Soedinenii. 2: 181–186.
  16. B. Bandgar; Makone, S. (2006). "Organic reactions in water. Transformation of aldehydes to nitriles using NBS under mild conditions". Synthetic Communications. 36 (10): 1347–1352. doi:10.1080/00397910500522009. S2CID 98593006.

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Binary compounds of hydrogen
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  • Transition metal hydrides
    Lanthanide hydrides
    Actinide hydrides
    Exotic matter hydrides
    Salts and covalent derivatives of the azide ion
    HN3 He
    LiN3 Be(N3)2 B(N3)3 CH3N3
    C(N3)4
    CO(N3)2
    NH4N3
    N3NO
    N(N3)3
    H2N–N3
    O FN3 Ne
    NaN3 Mg(N3)2 Al(N3)3 Si(N3)4 P SO2(N3)2 ClN3 Ar
    KN3 Ca(N3)2 Sc(N3)3 Ti(N3)4 VO(N3)3 Cr(N3)3
    CrO2(N3)2
    Mn(N3)2 Fe(N3)2
    Fe(N3)3
    Co(N3)2
    Co(N3)3
    Ni(N3)2 CuN3
    Cu(N3)2
    Zn(N3)2 Ga(N3)3 Ge As(N3)5 Se(N3)4 BrN3 Kr
    RbN3 Sr(N3)2 Y(N3)3 Zr(N3)4 Nb Mo Tc Ru(N3)6 Rh(N3)6 Pd(N3)2 AgN3 Cd(N3)2 In Sn Sb(N3)5 Te(N3)4 IN3 Xe(N3)2
    CsN3 Ba(N3)2 * Lu(N3)3 Hf Ta W Re Os Ir(N3)6 Pt(N3)6 Au(N3)4 Hg2(N3)2
    Hg(N3)2
    TlN3 Pb(N3)2 Bi(N3)3 Po At Rn
    Fr Ra(N3)2 ** Lr Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
     
    * La(N3)3 Ce(N3)3
    Ce(N3)4
    Pr Nd Pm Sm(N3)3 Eu(N3)2
    Eu(N3)3
    Gd(N3)3 Tb Dy(N3)3 Ho(N3)3 Er Tm Yb(N3)3
    ** Ac(N3)3 Th(N3)4 Pa UO2(N3)2 Np Pu Am Cm Bk Cf Es Fm Md No
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